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REVIEW article
Front. Cell Dev. Biol.
Sec. Signaling
Volume 12 - 2024 |
doi: 10.3389/fcell.2024.1462808
This article is part of the Research Topic Revolutionizing Cancer Treatment: Navigating the Intricate Landscape of Cellular Signaling Networks View all 8 articles
A stumbling block in pancreatic cancer treatment: drug resistance signaling networks
Provisionally accepted- 1 Dalian Medical University, Dalian, China
- 2 Westlake University, Hangzhou, Zhejiang, China
The primary node molecules in the cell signaling network in cancer tissues are maladjusted and mutated in comparison to normal tissues, which promotes the occurrence and progression of cancer. Pancreatic cancer (PC) is a highly fatal cancer with increasing incidence and low five-year survival rates. Currently, there are several therapies that target cell signaling networks in PC. However, PC is a "cold tumor" with a unique immunosuppressive tumor microenvironment (poor effector T cell infiltration, low antigen specificity), and targeting a single gene or pathway is basically ineffective in clinical practice. Targeted matrix therapy, targeted metabolic therapy, targeted mutant gene therapy, immunosuppressive therapy, cancer vaccines, and other emerging therapies have shown great therapeutic potential, but results have been disappointing. Therefore, we summarize the identified and potential drug-resistant cell signaling networks aimed at overcoming barriers to existing PC therapies.
Keywords: Pancreatic Cancer, signaling network, Drug Resistance, Matrix, gemcitabine
Received: 10 Jul 2024; Accepted: 30 Dec 2024.
Copyright: © 2024 Liu, Zhang, Huang, Zhang, Guo, Wang and Shang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Kexin Zhang, Dalian Medical University, Dalian, China
Fujia Guo, Dalian Medical University, Dalian, China
Zhizhou Wang, Dalian Medical University, Dalian, China
Dong Shang, Dalian Medical University, Dalian, China
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